Normative N1 audiogram data for the barbiturate-anaesthetised domestic cat.
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Acoustic Impedance Tests↗
Biomedical subjects
D R Irvine
Publications and source records attributed to D R Irvine.
The anterior ectosylvian sulcal auditory field in the cat: I. An electrophysiological study of its relationship to surrounding auditory cortical fields.
The extent of a region containing acoustically responsive neurons within the anterior ectosylvian sulcus and its relationship to surrounding gyral auditory cortical fields was examined in chloralose-anaesthetized cats. Multiple microelectrode penetrations were made orthogonal to the middle and anterior ectosylvian gyral surfaces, and longer penetrations were made into the dorsal and ventral banks and fundus of the anterior ectosylvian sulcus. The quantitative and qualitative auditory response characteristics of neurons and neuron clusters in the sulcal banks and surrounding regions were mapped in detail, and the degree of overlap of auditory and visual neurons within the sulcus was determined by routinely testing for responsiveness to a gross light flash. The detailed results from three animals and a summary of all penetrations into the sulcus are presented. The anterior ectosylvian sulcal field (Field AES) lay deep within the banks and fundus of the posterior three quarters of the sulcus. A combination of changes in the auditory response characteristics of neurons (i.e., in optimal stimulus, latency, and frequency tuning), and the presence of visually responsive cells, distinguished this field from surrounding fields. The distinction between the anterior ectosylvian field and extensions of the nearby tonotopic fields (i.e., primary and anterior auditory fields) into the dorsal and ventral banks of the dorsoposterior sector of the sulcus was readily made on the basis of these characteristics. The distinction between the anterior ectosylvian field and extensions of the second auditory field into the ventral bank of the middle sector of the sulcus was more difficult and there were differences between animals in the transition between these fields. Anterior ectosylvian sulcal field responses did not extend into the dorsal bank in anterior parts of the sulcus but were restricted to fundal regions, an observation consistent with the presence of the fourth somatosensory field in the dorsal bank of this sector of the sulcus. The majority of penetrations into the sulcus revealed coextensive auditory and visual activity, an observation apparently at variance with the identification of a purely visual field in this region. Barbiturate anaesthesia, which has been used in experiments demonstrating an anterior ectosylvian visual area, was found to have a depressing effect on auditory responses within the anterior ectosylvian sulcal field.
Acoustic Stimulation↗
The anterior ectosylvian sulcal auditory field in the cat: II. A horseradish peroxidase study of its thalamic and cortical connections.
The thalamic and cortical projections to acoustically responsive regions of the anterior ectosylvian sulcus were determined by identifying retrogradely labelled cells after physiologically guided iontophoretic injections of horseradish peroxidase. The medial division of the medial geniculate nucleus, the intermediate division of the posterior nuclear group, the principal division of the ventromedial nucleus, and the lateroposterior complex were consistently labelled after these injections, although each animal showed slightly different patterns of labelling. The suprageniculate nucleus and the lateral and medial divisions of the posterior nuclear group were also labelled in most experiments. The cortex of the suprasylvian sulcus was the most consistently and densely labelled cortical region; each experiment showed a slightly different pattern of labelling throughout the suprasylvian sulcus, with an overall tendency for greater labelling in the ventral (lateral) bank of the middle region of the sulcus. Other cortical regions labelled less consistently included the anterior ectosylvian sulcus itself, the insular cortex of the anterior sylvian gyrus, and the posterior rhinal sulcus. In three experiments the contralateral cortex was examined and a small number of labelled cells was located in the anterior ectosylvian and suprasylvian sulci. Input from extralemniscal auditory thalamus is compatible with previously described auditory response properties of anterior ectosylvian sulcus neurons. The results also confirm the presence of input from visual and multimodal regions of thalamus and cortex, and therefore support claims of overlap of modalities within the sulcus. This overlap, as well as input from motor regions, suggests that the anterior ectosylvian sulcal field serves a sensorimotor role.
Acoustic Stimulation↗
Binaural interaction in high-frequency neurons in inferior colliculus of the cat: effects of variations in sound pressure level on sensitivity to interaural intensity differences.
1. Development of models of the manner in which interaural intensity differences (IIDs), the major binaural cue for the azimuthal location of high-frequency sounds, are coded by populations of neurons requires knowledge of the extent to which the IID sensitivity of individual neurons is invariant with changes in sound pressure level (SPL) and other stimulus parameters. To examine this tissue, recordings were obtained from a large sample (n = 458) of neurons with characteristic frequency (CF) greater than 3 kHz in the central nucleus of the inferior colliculus (ICC) of anesthetized cats. The sensitivity to IIDs and the effects of changes in SPL on this sensitivity were examined in neurons receiving excitatory contralateral input and inhibitory or mixed inhibitory/facilitatory ipsilateral input (EI neurons). 2. The form of an EI neuron's IID sensitivity and the effects of changes in SPL on that sensitivity were found to be determined in part by the characteristics of the neuron's rate-intensity function for monaural contralateral stimulation, and detailed rate-intensity functions were therefore obtained for 91 neurons. Many ICC neurons have nonmonotonic rate-intensity functions, the proportion so classified depending on the criterion of nonmonotonicity employed. 3. IID sensitivity functions for CF tonal stimuli were obtained at one or more intensities for 90 neurons, using a method of generating IIDs that kept the average binaural intensity (ABI) of the stimuli at the two ears constant. In the standard ABI range in which a function was obtained for each unit, the majority of EI neurons (72%) had monotonic (sigmoidal) or near-monotonic IID sensitivity functions. The remainder had nonmonotonic (peaked) IID sensitivity functions, which were attributable either to mixed inhibitory and facilitatory ipsilateral influences or to the fact that the effects of ipsilateral stimulation were superimposed on nonmonotonic effects of changes in intensity at the excitatory ear. 4. IID sensitivity was examined at two or more ABIs (3-5 in most cases) for 40 neurons classified as having monotonic or near-monotonic functions in the standard ABI range and for 7 neurons classified as nonmonotonic. For a small proportion of neurons with monotonic IID sensitivity functions, the form of the function was relatively invariant with changes in ABI. In those monotonic neurons in which the form of the IID sensitivity function varied with changes in ABI, the most common type of variation was that the position of the sloping portion of the function shifted systematically in the direction of larger IIDs favoring the ipsilateral ear as ABI increased.(ABSTRACT TRUNCATED AT 400 WORDS)
Action Potentials↗
Azimuthal sensitivity of neurons in primary auditory cortex of cats. I. Types of sensitivity and the effects of variations in stimulus parameters.
1. Preliminary to studying the organization of azimuthal sensitivity of neurons along frequency-band strips in the primary auditory cortex (AI) of cat (see companion paper), this study examined the sensitivity of 251 units in cat AI to variations in the azimuthal location of sound sources in the frontal hemifield. Most units (231) were tested with tones at the characteristic frequency (CF; frequency to which the unit had the lowest threshold). Unit CFs ranged from 5 to 36 kHz. A large number of units (91) were tested with broadband noise stimuli, and a few units were also tested at other frequencies within the cell's tuning response area. 2. When tested at stimulus intensities 20-30 dB above CF or noise threshold, the different forms of azimuthal sensitivity exhibited by AI neurons could be divided into (1) contra-field azimuth functions; (2) ipsi-field functions; (3) central-field functions; (4) omnidirectional functions, and (5) multipeaked functions. Contra-field azimuth functions were the most prevalent, with 45.9% of units tested with CF tones and 42.9% of units tested with noise exhibiting this type of azimuthal sensitivity. Ipsi-field azimuthal sensitivity was found in 16.9% of units tested with CF tones and 19.8% of units tested with noise. Central-field azimuthal sensitivity was seen in 10.8% of units tested with CF tones and 17.6% of units tested with noise. Omnidirectional azimuthal sensitivity was seen in 19.9% of units tested with CF tones and 17.6% of units tested with noise, whereas multipeaked azimuthal sensitivity was found in 6.5% of units tested with CF tones and 5.5% of units tested with noise. 3. The effects of increasing stimulus intensity on azimuthal sensitivity were examined in 185 units tested with CF tones and 67 units tested with noise. For four major classes of azimuthal sensitivity (contra-field, ipsi-field, central-field and omnidirectional), the most common effect (approximately 60% of each class) was for the azimuth function to remain constant in form by the defining criteria for these classes. The next most common effect for all classes except omnidirectional azimuth functions was for an expansion of the azimuthal range eliciting responses. (The definition of omnidirectionality precluded any expansion of the response range in this class of azimuth function). A smaller number of units in some classes showed a compression of the azimuth function to a smaller response range, and others showed more complex expansive and compressive effects with increasing stimulus intensity.(ABSTRACT TRUNCATED AT 400 WORDS)
Acoustic Stimulation↗
Azimuthal sensitivity of neurons in primary auditory cortex of cats. II. Organization along frequency-band strips.
1. The organization of azimuthal sensitivity of units across the dorsoventral extent of primary auditory cortex (AI) was studied in electrode penetrations made along frequency-band strips of AI. Azimuthal sensitivity for each unit was represented by a mean azimuth function (MF) calculated from all azimuth functions obtained to characteristic frequency (CF) stimuli at intensities 20 dB or more greater than threshold. MFs were classified as contrafield, ipsi-field, central-field, omnidirectional, or multipeaked, according to the criteria established in the companion paper (Rajan et al. 1990). 2. The spatial distribution of three types of MFs was not random across frequency-band strips: for contra-field, ipsi-field, and central-field MFs there was a significant tendency for clustering of functions of the same type in sequentially encountered units. Occasionally, repeated clusters of a particular MF type could be found along a frequency-band strip. In contrast, the spatial distribution of omnidirectional MFs along frequency-band strips appeared to be random. 3. Apart from the clustering of MF types, there were also regions along a frequency-band strip in which there were rapid changes in the type of MF encountered in units isolated over short distances. Most often such changes took the form of irregular, rapid juxtapositions of MF types. Less frequently such changes appeared to show more systematic changes from one type of MF to another type. In contrast to these changes in azimuthal sensitivity seen in electrode penetrations oblique to the cortical surface, much less change in azimuthal sensitivity was seen in the form of azimuthal sensitivity displayed by successively isolated units in penetrations made normal to the cortical surface. 4. To determine whether some significant feature or features of azimuthal sensitivity shifted in a more continuous and/or systematic manner along frequency-band strips, azimuthal sensitivity was quantified in terms of the peak-response azimuth (PRA) of the MFs of successive units and of the azimuthal range over which the peaks occurred in the individual azimuth functions contributing to each MF (the peak-response range). In different experiments shifts in these measures of the peaks in successively isolated units along a frequency-band strip were found generally to fall into one of four categories: 1) shifts across the entire frontal hemifield; 2) clustering in the contralateral quadrant; 3) clustering in the ipsilateral quadrant; and 4) clustering about the midline. In two cases more than one of these four patterns were found along a frequency-band strip.(ABSTRACT TRUNCATED AT 400 WORDS)
Acoustic Stimulation↗
Plasticity of frequency organization in auditory cortex of guinea pigs with partial unilateral deafness.
We have examined the effect of restricted unilateral cochlear lesions on the orderly topographic mapping of sound frequency in the auditory cortex of adult guinea pigs. These lesions, although restricted in spatial extent, resulted in a variety of patterns of histological damage to receptor cells and nerve fibres within the cochlea. Nevertheless, all lesions resulted in permanent losses of sensitivity of the cochlear neural output across a limited frequency range. Thirty-five to 81 days after such damage to the organ of Corti, the area of contralateral auditory cortex in which the lesioned frequency range would normally have been represented was partly occupied by an expanded representation of sound frequencies adjacent to the frequency range damaged by the lesion. The thresholds at their new characteristic frequencies (CFs) of clusters of cortical neurones in these regions were close to normal thresholds at those frequencies (mean difference across all animals was 3.8 dB). In a second series of experiments, the responses of neurone clusters were examined within hours of making similar cochlear lesions. It was found that shifts in CF toward frequencies spared by the lesions could occur, but thresholds were greatly elevated compared to normal (mean difference was 31.7 dB in five animals). The emergence of sensitive drive in such regions after prolonged recovery periods in lesioned animals thus suggests that the auditory cortical frequency map undergoes reorganization in cases of partial deafness. Some features of this reorganization are similar to changes reported in somatosensory cortex after peripheral nerve injury, and this form of plasticity may therefore be a feature of all adult sensory systems.
Animals↗
Connections of the primary auditory cortex in the common marmoset, Callithrix jacchus jacchus.
The afferent and efferent connections of the primary auditory cortex (AI) of common marmosets were traced following small injections of wheat germ agglutinin conjugated with horseradish peroxidase (WGA-HRP) made at best frequency (BF)-defined sites in the AI. After the injections the animals remained anesthetized for 15-23 hours; they were then perfused transcardially with fixative and the brains were processed for WGA-HRP reaction product. Examination of the disposition of labelled material revealed the following results. First, patches of terminal labelling, and to a lesser extent retrograde labelling, were found outside the injection site in the ipsilateral cortex rostral and caudal to the AI. Second, the region of the contralateral cortex corresponding to the injection site contained labelled terminals throughout the depth of the cortex; labelled neurons were found in the middle layers. Third, in each experiment a discrete region of the medial geniculate body (MG) contained retrogradely labelled neurons interspersed with anterogradely labelled terminals. These regions had a banded appearance, were found in the dorsal and rostral half of the MG, and shifted in location progressively dorsalward as the injection site BF increased. The presence of projection zones rostral and caudal to the AI of marmosets, and the disposition of the MG sources of projection in relation to BF, are similar to observations made on other New World monkeys. The ipsilateral corticocortical projections confirm electrophysiological evidence suggesting the existence of auditory fields rostral and caudal to the AI. The thalamocortical auditory system of the marmoset appears relatively simple, with a comparatively undifferentiated MG projecting to a cortical auditory system dominated by a large AI.
Animals↗
Interaural intensity differences in the cat: changes in sound pressure level at the two ears associated with azimuthal displacements in the frontal horizontal plane.
The changes in sound pressure level (SPL) at the two ears produced by azimuthal displacements of a free-field sound source in the interaural horizontal plane in frontal space were measured in anesthetized cats and the resultant interaural intensity differences (IIDs) were derived by subtraction. The mean curves at different frequencies indicate that azimuthal displacements from the median sagittal plane are generally associated with increases in SPL at the near (directly irradiated) ear and decreases at the far (shadowed) ear. Detailed measurements at 1 degree and 2 degrees azimuthal steps in some animals revealed that at frequencies above 6-8 kHz there were marked variations in tympanic SPL at the far ear at lateral azimuths; these variations are apparently produced by interference between sets of 'creeping' surface waves propagated around the head in each direction. Near-ear changes were generally non-monotonic, becoming smaller or, in some cases, negative at large azimuthal displacements. At some frequencies above 8-10 kHz, functions for individual animals exhibited sharp decreases in level at the near ear (and consequently negative IIDs) at small azimuthal displacements. The general characteristics of the near-ear changes are in accord with previous evidence on the directionality of pinna amplification effects, although the sharp notches at some frequencies and azimuths presumably reflect more complex resonance and interference phenomena. Differences in the IID-azimuth relationship at different frequencies correlate well with data on the acuity of localization of high-frequency tones by cats.
Acoustic Stimulation↗
A comparison of two methods for the measurement of neural sensitivity to interaural intensity differences.
Two alternative methods for the measurement of neural sensitivity to interaural intensity differences (IIDs) were used to obtain IID-sensitivity functions for samples of excitatory-inhibitory (EI) neurons from the central nucleus of the inferior colliculus and the primary auditory cortex of the cat. In one, the EMI-constant method, intensity was held constant in the ear providing excitatory input and varied above and below that level in the other ear. In the alternative (ABI-constant) method, intensity at the two ears was varied symmetrically about a constant base intensity, in a manner roughly approximating the pattern of changes that occur when a free-field stimulus is moved in azimuth from the median sagittal plane. For neurons with monotonic or near-monotonic rate-intensity functions for the excitatory ear, the two methods generated IID-sensitivity functions that were identical or near-identical by a number of quantitative criteria. For neurons with non-monotonic rate-intensity functions, however, the IID functions generated by the two methods were very different: those produced by the EMI-constant method were monotonic, whereas those generated by the ABI-constant method were non-monotonic and sharply peaked. The advantages and disadvantages of the two methods, and the implications of the results for the neural encoding of IIDs and for the azimuthal sensitivity of EI neurons with non-monotonic rate-intensity functions, are discussed.
Animals↗
Auditory response properties of neurons in the anterior ectosylvian sulcus of the cat.
The auditory response properties of single neurons in the fundus and banks of the anterior ectosylvian sulcus (AES) were studied with simple dichotic stimuli (viz. noise- and tone-bursts) in cats anaesthetized with alpha-chloralose. Neurons within AES showed simple onset responses, were most commonly excited by stimulation of both ears, and showed either broad tuning or multiple high best frequencies. Some neurons were also tested for visual responsiveness and it was found that auditory cells and visual cells were intermingled within the sulcus. A small percentage of cells responded to both auditory and visual stimulation. Overall, the response properties of AES neurons differed from those of nearby auditory cortical fields. The region of AES studied appears to be outside the recently defined fourth somatosensory area (SIV), but overlaps para-SIV found deeper in the sulcus. It appears that deep within the sulcus and along most of its length there is a population of auditory, somatosensory and visual cells; to delineate this auditory population from the surrounding auditory cortical fields this region has been designated Field AES.
Animals↗
Frequency representation in auditory cortex of the common marmoset (Callithrix jacchus jacchus).
The location and characteristics of the primary auditory cortex of the common marmoset, Callithrix jacchus jacchus, were determined in five anesthetized male adult animals by mapping the responses of cortical units and unit clusters to pure tone stimuli presented to the contralateral ear. The primary auditory cortex lies largely ventral to the lateral sulcus, the only major fissure on the lateral cortex of this smooth-brained primate, but in some animals it may extend significantly down the ventral bank of this sulcus. Responses are distributed such that low best frequencies are found rostroventrally whereas high best frequencies occur caudally. The disposition of frequency-band contours is fan-shaped, with contours separating low-frequency octaves nearly parallel to the lateral sulcus and high-frequency (greater than 8 kHz) contours perpendicular to that sulcus. Best frequencies range from 0.6 to 30 kHz across the primary field, but there is a disproportionate representation of the three octaves between 2 and 16 kHz. The most sensitive thresholds (as low as -2 dB SPL) are found between 7 and 9 kHz. The primary auditory cortex is similar in cytoarchitecture to that reported for the cat, showing a blurring of lamination in the middle layers (II-IV) and a preponderance of small cells in these merged layers, giving a highly granular appearance. The accessibility of the cochlear representation on the gyral surface makes the marmoset an attractive animal for studies of primate auditory cortex.
Animals↗
Auditory response properties of neurons in the claustrum and putamen of the cat.
The auditory response properties of single neurons in claustrum and putamen were studied in response to simple dichotic stimuli (viz. noise-and tone-bursts) in chloralose-anaesthetized cats. Neurons in claustrum were commonly weakly driven with long latency, were broadly tuned and were excited by stimulation of either ear (EE). Putamen neurons, in contrast, were securely driven with short latency, showed irregular tuning with a preference for low frequencies and were either EE or excited only by the contralateral ear (EO). The differences between claustrum and putamen responses can be related to differences in connections with the auditory cortical fields and with auditory thalamus. Some neurons were also tested for visual responsiveness: auditory and visual cells were intermingled in both nuclei and only a small percentage of cells were bimodal. In contrast to the visual and somatosensory input to claustrum, which are derived from primary cortical fields, the auditory input to claustrum is apparently derived from non-primary cortical regions, suggesting a fundamentally different role for processing of auditory information in claustrum.
Animals↗
Effects of interaural time delays of noise stimuli on low-frequency cells in the cat's inferior colliculus. I. Responses to wideband noise.
We examined the responses of low-frequency neurons in the central nucleus of the inferior colliculus (ICC) of the cat to interaurally delayed, wideband noise stimuli. The stimuli were pseudorandom noise signals that were generated digitally with a nominal bandwidth of 60-4,000 Hz. We also compared the responses to noise with those obtained from interaural phase differences of pure tones. We studied 144 neurons with characteristic frequencies below 2.5 kHz. Eighty-five percent (85%) of these were sensitive to changes in both interaural time differences (ITDs) of noise and interaural phase differences of pure tones, only 2% were sensitive to one stimulus but not the other, and the remainder were insensitive to both stimuli. For most cells the discharge rate was modulated in an approximately cyclic fashion by changes in ITDs of the wideband noise stimuli. The maximal spike counts often occurred near zero ITD, and there was considerable variability in the nature of the cycling, though it usually disappeared for ITDs greater than +/- 4,000 microseconds. The position of the central peak was usually (65%) within the physiologically relevant range of +/- 400 microseconds, and most (80%) occurred at positive ITDs, which corresponded to delays to the ipsilateral stimulus. In general, the shapes of the responses were not affected by changes in stimulus level above threshold. As long as identical noises were delivered to both ears, the responses were not sensitive to the particular noise stimulus used. When uncorrelated noises were delivered to the two ears, there was no sensitivity to ITDs. Composite curves were computed by linear summation of the responses to ITDs of pure tones at frequencies spaced at equal intervals throughout each cell's response area. The shapes of composite curves were similar to the responses of the same cell to ITDs of wideband noise stimuli. The positions of the central peaks of these two functions were highly correlated (r = 0.91, slope = 0.97). The values of characteristic delay and characteristic phase computed from the tonal responses were found to be good indicators of the shapes of the noise delay curves. Characteristic phases (CPs) near zero were associated with noise delay curves symmetric about the central peak, CPs near 0.5 cycles with those symmetric about the trough, while CPs between 0 and 0.5 or between 0.5 and 1.0 had noise delay curves that were asymmetric with a prominent trough to the left or right, respectively, of the central peak.(ABSTRACT TRUNCATED AT 400 WORDS)
Animals↗
Frequency representation in the auditory midbrain and forebrain of a marsupial, the northern native cat (Dasyurus hallucatus).
The representation of sound frequency was examined in the auditory cortex and inferior colliculus of anaesthetized marsupial native cats (Dasyurus hallucatus) using microelectrode mapping techniques. The tonotopic organizations of these two auditory regions are grossly similar to those described in brush-tailed possums and in Eutheria. There appears to exist a biased representation of high frequencies (greater than 10kHz) in native cats and a paucity of frequencies below 1 kHz. Unit threshold audiograms indicate minimum thresholds between 7 and 12kHz and high thresholds above 30kHz.
Animals↗
Topographic organization of interaural intensity difference sensitivity in deep layers of cat superior colliculus: implications for auditory spatial representation.
Sensitivity to interaural intensity difference (IID) was examined for 103 neurons in the deep layers of superior colliculus (SC) in ketamine barbiturate-anesthetized cats. Noise stimuli were presented dichotically, and IID sensitivity functions were generated while keeping the average binaural intensity (ABI) of stimulation constant. Neurons of three binaural classes were found to be IID sensitive. Neurons receiving excitatory contralateral input and inhibitory ipsilateral input (EO/I cells, 55% of sample) had steplike IID functions, with maximum response at IIDs corresponding to contralateral azimuths (positive IIDs), total suppression at IIDs corresponding to ipsilateral azimuths (negative IIDs), and cutoffs at different positions along the IID axis for different neurons. Neurons responsive only to binaural stimulation (OO/F cells, 15% of sample) had IID functions with a sharp peak in the range of 0 to 10 dB IID. Cells receiving excitatory input contralaterally and a facilitatory ipsilateral input (EO/F cells, 7% of sample) had IID functions of intermediate shape, with a peak in the range of 10 to 20 dB IID and a sharper cutoff near zero IID than at larger positive IIDs. The sharpness of IID cutoff for EO/I cells was quantified by measuring an 80% IID dynamic range. Neurons with 80% IID dynamic ranges of less than 26 dB were judged to have sharp cutoffs. The position along the IID axis of the IID cutoff for these cells was quantified by recording the IID at which the response was at 50% of maximum (half-maximal IID). A topographic organization of EO/I cells with sharp IID cutoffs was found along the rostrocaudal axis of SC, such that rostral EO/I cells had IID functions with half-maximal IIDs near zero, while increasingly caudal EO/I cells had progressively larger (positive) half-maximal IIDs. Although detailed maps could not be obtained in individual animals, the topography was observed in each of nine experiments in which EO/I cells were located in two or more rostrocaudal locations (P = 0.00002). The effect of stimulus level on the stability of IID cutoff was examined for 13 EO/I cells. The majority (85%) showed less than 10 dB variation in half-maximal IID across a range of suprathreshold ABIs, indicating that EO/I cells in SC generally exhibit stability in cutoff with changes in intensity of broadband stimuli.(ABSTRACT TRUNCATED AT 400 WORDS)
Animals↗
Interaural intensity difference sensitivity based on facilitatory binaural interaction in cat superior colliculus.
Sensitivity to interaural intensity difference (IID) has generally been identified as a property of neurons exhibiting inhibitory binaural interaction, viz. contralateral excitatory and ipsilateral inhibitory input (EI cells). In the deep layers of the superior colliculus, however, almost 30% of IID-sensitive cells are characterised by facilitatory or mixed facilitatory/inhibitory interactions. Such cells typically have peaked IID sensitivity functions in contrast to the step functions characteristic of EI cells. There appears to be a continuum in IID sensitivity from pure step functions to sharply-peaked functions. The observation that a given form of IID sensitivity can be associated with patterns of binaural interaction other than that by which it is most commonly produced suggests that IID-sensitive neurons are better classified on the basis of the form of their IID sensitivity than their binaural input pattern. It seems probable that IID sensitivity based on facilitatory and mixed facilitatory/inhibitory binaural interactions is a general characteristic of the primary auditory pathway, although only fragmentary data are so far available.
Animals↗
Masking by internally generated noise and protection by middle ear muscle activity.
Gross auditory nerve action potentials to high-frequency clicks were recorded bilaterally from awake cats with unilaterally tenotomized middle ear muscles (MEM) during eating and during control quiet periods. Masking by internally generated noise associated with eating increased with decreases in click intensity, but did not differ in ears with intact and tenotomized MEM. Under the conditions of this study, non-reflex MEM activity does not appear to provide protection against masking by internally generated noise.
Action Potentials↗